<p>Copper ions (Cu<sup>2+</sup>) are essential in numerous biological and environmental processes, yet their excess can lead to severe toxicity. Hence, developing selective and sensitive colorimetric sensors for Cu<sup>2+</sup> detection remains a critical research pursuit. In this study, a newly synthesized Nin–PyHz-based chemosensor, 2-(2-(pyridin-2-yl)hydrazono)-1H-indene-1,3(2&#xa0;H)-dione (<b>L</b>), was explored for its selective Cu<sup>2+</sup> recognition ability. The sensor exhibited a distinct optical response exclusively toward Cu<sup>2+</sup> ions, while other metal ions and anions caused negligible interference. The free ligand showed an absorption band at 382&#xa0;nm, which shifted to 434&#xa0;nm upon Cu<sup>2+</sup> binding, accompanied by a perceptible color change, indicating complex formation. This bathochromic shift arises from modulation of the intramolecular charge transfer (ICT) process upon coordination with Cu<sup>2+</sup> ions. The binding constant, derived from the Benesi–Hildebrand relation, was found to be 1.83 × 10<sup>5</sup> M⁻<sup>1</sup>, and the limit of detection (LOD) was determined as 0.69 µM. Job’s plot confirmed a 1:1 stoichiometric interaction between <b>L</b> and Cu<sup>2+</sup> ions. The sensor exhibited optimal performance in the pH range of 6.0–8.0, highlighting its excellent selectivity and applicability for Cu<sup>2+</sup> detection in real or complex samples.</p>

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A simple ninhydrin–hydrazone probe for highly selective and sensitive colorimetric detection of Cu2+ ions

  • Vanie V,
  • Kavitha R

摘要

Copper ions (Cu2+) are essential in numerous biological and environmental processes, yet their excess can lead to severe toxicity. Hence, developing selective and sensitive colorimetric sensors for Cu2+ detection remains a critical research pursuit. In this study, a newly synthesized Nin–PyHz-based chemosensor, 2-(2-(pyridin-2-yl)hydrazono)-1H-indene-1,3(2 H)-dione (L), was explored for its selective Cu2+ recognition ability. The sensor exhibited a distinct optical response exclusively toward Cu2+ ions, while other metal ions and anions caused negligible interference. The free ligand showed an absorption band at 382 nm, which shifted to 434 nm upon Cu2+ binding, accompanied by a perceptible color change, indicating complex formation. This bathochromic shift arises from modulation of the intramolecular charge transfer (ICT) process upon coordination with Cu2+ ions. The binding constant, derived from the Benesi–Hildebrand relation, was found to be 1.83 × 105 M⁻1, and the limit of detection (LOD) was determined as 0.69 µM. Job’s plot confirmed a 1:1 stoichiometric interaction between L and Cu2+ ions. The sensor exhibited optimal performance in the pH range of 6.0–8.0, highlighting its excellent selectivity and applicability for Cu2+ detection in real or complex samples.